Banwell, Martin - 暨南大学 - 先进与应用化学合成研究院

个人简介

Academician and Professor Martin Banwell is an internationally renowned expert in organic chemistry. He is now the Dean of Institute for Advanced and Applied Chemical Synthesis (IAACS) as well as a Master/PhD tutor, and his main study is the total synthesis of active natural products and research and development of new drugs. He was elected as an academician of Australian Academy of Sciences in 2004, and he is also a fellow of the Royal Society of Chemistry and the Royal Australian Chemical Society, as well as an honorary fellow of the Royal New Zealand Chemical Society. He was a highest-level (Level-E2) tenure-track professor at the Australian National University. In 2018, he was awarded the Officer Medal by the Australian Federal Government, the highest level award for Australian citizens, for his contribution in scientific research. In 2021, he was awarded the Chinese Government Friendship award by the Prime Minister Keqiang Li. Till now, he has published almost 400 SCI papers on journals like Nature Chemistry, Accounts of Chemical Research, and Organic Letters, and he was authorized for 13 international patents. Education& Professional Experience 2020–present Dean, Institute for Advanced and Applied Chemical Synthesis, Jinan University 2013–2019 Professor Research School of Chemistry, Australian National University 2008–2013 Dean Research School of Chemistry, Australian National University 1977–1979 PhD (Specialty: Material chemistry) Victoria University of Wellington, New Zealand 1976–1977 Master of Science (Specialty: Material chemistry) Victoria University of Wellington, New Zealand 1972–1976 Bachelor of Science (Specialty: Material chemistry) Victoria University of Wellington, New Zealand

研究领域

his main study is the total synthesis of active natural products and research and development of new drugs.

近期论文

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White, L. V., Hu, N., He, Y. T., Banwell, M. G.*, & Lan, P.* Expeditious Access to Morphinans by Chemical Synthesis. Angew. Chem. Int. Ed.2022, e202203186 (IF: 15.336，Level A1) Chen, Y., Lan, P.*, & Banwell, M. G.* Total Synthesis of Denigrin E and Its Oxidative Conversion into Co-occurring Metabolite Denigrin D. Org. Lett.2022, 24, 2931–2934. (IF: 6.005，Level A1) Banwell, M. G.*; Liu, X.; Connal, L. A.; Gardiner, M. G. Synthesis of Functionally and Stereochemically Diverse Polymers via Ring-Opening Metathesis Polymerization of Derivatives of the Biomass-derived Platform Molecule Levoglucosenone Produced at Industrial Scale. Macromolecules2020, 53, 5308–5314. (IF: 5.985，Level A1) Sheng, B.; Vo, Y.; Lan, P.; Gardiner, M. G.; Banwell, M. G.*; Sun, P.* Direct and metal-catalyzed photochemical dimerization of the phthalide (Z)-ligustilide leading to both [2 + 2] and [4 + 2] cycloadducts: application to total syntheses of tokinolides A-C and riligustilide. Org. Lett.2019, 21, 6295–6299. (IF: 6.005，Level A1) Khan, F.; Fatima, M.; Shirzaei, M.; Vo, Y.; Amarasiri, M.; Banwell, M. G.*; Ma, C.; Ward, J. S.; Gardiner, M. G. Tandem Ullmann-Goldberg cross-coupling/cyclopalladation-reductive elimination reactions and related sequences leading to polyfunctionalized benzofurans, indoles, and phthalanes. Org. Lett.2019, 21, 6342–6346. (IF: 6.005，Level A1) Mikusek, J.; Nugent, J.; Ward, J. S.; Schwartz, B. D.; Findlay, A. D.; Foot, J. S.; Banwell, M. G.* Synthetic Studies on the Natural Product Myrsinoic Acid F Reveal Biologically Active Analogues. Org. Lett.2018, 20, 3984–3987. (IF: 6.005，Level A1) Khan, F.; Dlugosch, M.; Liu, X.; Banwell, M. G.*. The Palladium-Catalyzed Ullmann Cross-Coupling Reaction: A Modern Variant on a Time-Honored Process. Accounts Chem. Res.2018, 51, 1784–1795. (IF: 23.384，Level A1) Khan, F.; Dlugosch, M.; Liu, X.; Khan, M.; Banwell, M. G.*; Ward, J. S.; Carr, P. D. Palladium-Catalyzed Ullmann Cross-Coupling of β-Iodoenones and β-Iodoacrylates with o-Halonitroarenes or o-Iodobenzonitriles and Reductive Cyclization of the Resulting Products To Give Diverse Heterocyclic Systems. Org. Lett. 2018, 20, 2770–2773. (IF: 6.005，Level A1) Ma, X.; Yan, Q.; Banwell, M. G.*; Ward, J. S. A Total Synthesis of the Antifungal Deoxyaminocyclitol Nabscessin B from L- (+)-Tartaric Acid. Org. Lett. 2018, 20, 142–145. (IF: 6.005，Level A1)